Design of Highly Electrophilic and Stable Metal Nitrido Complexes

ConspectusMetal oxo (M═O) and nitrido (M≡N) complexes are two important classes of high-valent transition metal complexes. The use of M═O as oxidants in chemical and biological systems has been extensively investigated. Nature makes use of M═O in enzymes such as cytochrome P450 to oxidize a variety of substrates. Highly oxidizing oxo species have also been synthesized and they have been shown to oxidize organic and inorganic substrates via one-electron oxidation, O atom transfer, and H atom abstraction pathways. In contrast, the oxidation chemistry of M≡N is much less investigated. Although a variety of nitrido complexes are known, most of them are inert and do not show appreciable oxidizing properties, which is not unexpected since the N3– ligand is much more electron-donating than the O2– ligand. In principle, highly electrophilic/oxidizing nitrido complexes may be designed by using weakly coordinating ancillary ligands and/or by increasing the oxidation state of the metal centers. A number of such species have been generated in solution at low temperatures. However, attempts to isolate them are often hampered by their ease of decomposition via bimolecular N···N coupling to generate N2. In some cases, decomposition occurs by intramolecular nitrogenation of the ancillary ligand.In this account, we describe our recent efforts into the design of nitrido complexes that are highly oxidizing but stable enough so they can be isolated and characterized, and their reactivity toward organic substrates can be readily investigated.We have successfully isolated and determined the structure of the first stable manganese(VI) nitrido complex bearing an oxidation-resistant macrocyclic tetraamido TAML ligand, MnVI(N)(TAML)− (H4TAML = 3,3,6,6,9,9-hexamethyl-3,4,8,9-tetrahydro-1H-benzoe1,4,7,10 tetraazacyclotridecine-2,5,7,10(6H,11H)-tetraone). This complex readily undergoes direct aziridination of alkenes; it also abstracts hydrides from NADH analogues via a Separated CPET mechanism. Coupling of the nitrido ligands to give dinitrogen is a major decomposition pathway for electrophilic nitrido complexes. In order to shut down this pathway, we made use of a bulky trianionic corrole ligand TTPPC (H3TTPPC = 5,10,15-tris(2,4,6-triphenylphenyl)corrole) to prepare manganese nitrido complexes. Remarkably, we were able to isolate and determine the structures of MnV(N)(TTPPC)− and its one- and two-electron ligand-oxidized products, MnV(N)(TTPPC+•) and MnV(N)(TTPPC2+)+ ("TTPPC" has a 3- charge, 'TTPPC+•' has an overall 2- charge and 'TTPPC2+' has an overall 1- charge). Although MnV(N)(TTPPC2+)+ is formally a manganese(V) complex, it was found to be the most electrophilic among isolated metal nitrido complexes. The use of the bulky corrole ligand effectively prevents the decomposition of Mn≡N by N···N coupling.A number of luminescent M═O species that possess highly oxidizing excited states are known. We have also developed a strongly luminescent osmium(VI) nitrido complex, OsVI(N)(L)(CN)3− (OsN, HL = 2-(2-hydroxy-5-nitrophenyl)benzoxazole), that absorbs visible light to generate a highly oxidizing/electrophilic excited state. The excited state readily reacts with a wide variety of organic and inorganic substrates, many of these reactions are unprecedented. Notably, it reacts with cyclohexane to give an osmium(IV) cyclohexyliminato product, and with benzene to give an osmium(IV) p-benzoquinone iminato species.